Found: 26
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A recurrent inactivating mutation in RHOA GTPase in angioimmunoblastic T cell lymphoma.
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- Nature Genetics, 2014, v. 46, n. 4, p. 371, doi. 10.1038/ng.2916
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Converging on neurodegenerative mechanisms.
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- Nature Genetics, 2014, v. 46, n. 4, p. 317, doi. 10.1038/ng.2954
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- Article
Inflammatory syndrome ADA2 deficiency.
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- Nature Genetics, 2014, v. 46, n. 4, p. 325, doi. 10.1038/ng.2943
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Recurrent somatic mutations of PTPN1 in primary mediastinal B cell lymphoma and Hodgkin lymphoma.
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- Nature Genetics, 2014, v. 46, n. 4, p. 329, doi. 10.1038/ng.2900
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Mutations in TJP2 cause progressive cholestatic liver disease.
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- Nature Genetics, 2014, v. 46, n. 4, p. 326, doi. 10.1038/ng.2918
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Recurrent PTPRB and PLCG1 mutations in angiosarcoma.
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- Nature Genetics, 2014, v. 46, n. 4, p. 376, doi. 10.1038/ng.2921
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Transmission of mitochondrial mutations and action of purifying selection in Drosophila melanogaster.
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- Nature Genetics, 2014, v. 46, n. 4, p. 393, doi. 10.1038/ng.2919
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PRKCI and SOX2 drive lung cancer.
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- Nature Genetics, 2014, v. 46, n. 4, p. 325, doi. 10.1038/ng.2946
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Zinc transport and diabetes risk.
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- Nature Genetics, 2014, v. 46, n. 4, p. 323, doi. 10.1038/ng.2934
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Mutations in the DNA methyltransferase gene DNMT3A cause an overgrowth syndrome with intellectual disability.
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- Nature Genetics, 2014, v. 46, n. 4, p. 385, doi. 10.1038/ng.2917
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Two pathways for courtship behavior.
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- Nature Genetics, 2014, v. 46, n. 4, p. 325, doi. 10.1038/ng.2944
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Ancient human oral plaque preserves a wealth of biological data.
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- Nature Genetics, 2014, v. 46, n. 4, p. 321, doi. 10.1038/ng.2930
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A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP.
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- Nature Genetics, 2014, v. 46, n. 4, p. 380, doi. 10.1038/ng.2899
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Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
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- Nature Genetics, 2014, v. 46, n. 4, p. 357, doi. 10.1038/ng.2915
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Systematic evaluation of coding variation identifies a candidate causal variant in TM6SF2 influencing total cholesterol and myocardial infarction risk.
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- Nature Genetics, 2014, v. 46, n. 4, p. 345, doi. 10.1038/ng.2926
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Promoter silencing by CGG repeats.
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- Nature Genetics, 2014, v. 46, n. 4, p. 325, doi. 10.1038/ng.2942
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Chalk5 encodes a vacuolar H<sup>+</sup>-translocating pyrophosphatase influencing grain chalkiness in rice.
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- Nature Genetics, 2014, v. 46, n. 4, p. 398, doi. 10.1038/ng.2923
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eQTL mapping for innate immunity.
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- Nature Genetics, 2014, v. 46, n. 4, p. 325, doi. 10.1038/ng.2945
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Global optimization of somatic variant identification in cancer genomes with a global community challenge.
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- Nature Genetics, 2014, v. 46, n. 4, p. 318, doi. 10.1038/ng.2932
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An epigenetic mechanism of resistance to targeted therapy in T cell acute lymphoblastic leukemia.
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- Nature Genetics, 2014, v. 46, n. 4, p. 364, doi. 10.1038/ng.2913
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RHOA mutations in peripheral T cell lymphoma.
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- Nature Genetics, 2014, v. 46, n. 4, p. 320, doi. 10.1038/ng.2937
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Direct measurement of transcription factor dissociation excludes a simple operator occupancy model for gene regulation.
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- Nature Genetics, 2014, v. 46, n. 4, p. 405, doi. 10.1038/ng.2905
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Selective propagation of functional mitochondrial DNA during oogenesis restricts the transmission of a deleterious mitochondrial variant.
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- Nature Genetics, 2014, v. 46, n. 4, p. 389, doi. 10.1038/ng.2920
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Ancestry estimation and control of population stratification for sequence-based association studies.
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- Nature Genetics, 2014, v. 46, n. 4, p. 409, doi. 10.1038/ng.2924
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Pathogens and host immunity in the ancient human oral cavity.
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- Nature Genetics, 2014, v. 46, n. 4, p. 336, doi. 10.1038/ng.2906
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Exome-wide association study identifies a TM6SF2 variant that confers susceptibility to nonalcoholic fatty liver disease.
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- Nature Genetics, 2014, v. 46, n. 4, p. 352, doi. 10.1038/ng.2901
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